Our client, a leading pharmaceutical company, seeks a Product Validation Manager with 5+ years of experience validating Class A cleanroom equipment. As the Product Validation Manager, you will oversee the operations of the day-to-day product quality assurance/validation programs and develop/implement systems/procedures that ensure products meet specifications while complying with GxP regulations. The position requires a Bachelor's Degree or higher in Engineering, Chemistry, Biology, or a related field, as well as knowledge of Quality engineering principles, including CSV.
Qualifications: - Bachelor's Degree or higher in Engineering, Chemistry, Biology, or related field. - 5+ years experience validating Class A cleanroom equipment - Experience managing product quality and process validation activities - Knowledge of Quality engineering principles, including CSV
Responsibilities: - Overseeing day-to-day operations associated with the product quality assurance/validation program(s). - Develop/implement systems/procedures that assure products manufactured at this location consistently meet specifications while complying with w/GxP regulations/guidance documents applicable across global markets where they/distributed - Responsible for providing oversight on execution/completion-validation deliverables per approved timelines/budget constraints. - Collaborate closely with w/Cross-functional teams consisting of experts/stakeholders responsible, e.g., Regulatory Affairs/QA-QC /Supply Chain/R&D-SME) - Ensuring timely completion/submission/approval-documentation relating data/reports generated during the entire lifecycle-product-development right from conception till commercialization stage
If you possess these qualifications/skills and desire a challenging role, please submit your application today!
EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
To find out more about Real, please visit www.realstaffing.com
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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